Down Syndrome Alabama was founded in June of 1987 by a small group of dedicated parents who came together with a shared purpose: to advocate for their children with Down syndrome and to ensure they had access to opportunity, support, and acceptance. At a time when resources were limited and awareness was still growing, these parents recognized the power of collective advocacy and community. They incorporated the organization under the name PADS (Parent Advocates Down Syndrome), establishing a formal structure that allowed their voices to be heard more broadly. 

In August of 2012, the Board of Directors made and seconded a motion to permanently change the organization’s name to Down Syndrome Alabama, reflecting a clearer identity and a broader statewide vision. On April 23, 2013, the amendment was officially filed, formally establishing Down Syndrome Alabama as the organization’s name and signaling an intentional step forward in its growth and mission.

In 2025, we are a forward-focused organization, built on strong governance, sound financial oversight, and clear strategic direction. We're evolving from a period of rebuilding into a season of growth, expanding programs, deepening partnerships, and strengthening its statewide reach. With updated bylaws, effective systems, and leadership aligned with best-practice governance and term limits, DSA is well positioned for long-term sustainability and impact. The organization now stands confident in its ability to serve individuals with Down syndrome and their families across Alabama, at every age, stage, and region.